Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 1
rs470117
CPT1B ; CHKB-CPT1B
1.000 0.040 22 50571524 missense variant C/T snv 0.42 0.36 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs4846922
GALNT2
1.000 0.040 1 230171436 intron variant T/A;C;G snv 1
rs3757840
GCK
1.000 0.040 7 44191617 intron variant T/C;G snv 1
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs7849191
JAK2
0.882 0.120 9 4988761 intron variant C/T snv 0.50 1
rs163182
KCNQ1
0.882 0.160 11 2822986 intron variant G/A;C snv 1
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs496300
LINC01679
1.000 0.040 21 43359800 intron variant C/T snv 0.73 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 1
rs2000813
LIPG
0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 1
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 1
rs295
LPL
1.000 0.040 8 19958727 intron variant A/C snv 0.28 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2293855
MTMR9
0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 1
rs10838681
NR1H3
1.000 0.040 11 47253513 intron variant G/A snv 0.34 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs782590
PPP4R3B ; LOC107985885
1.000 0.040 2 55616277 intron variant C/T snv 0.44 1
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 1
rs4923918
SPTBN5
0.882 0.160 15 41868745 intron variant G/A snv 4.1E-02 1
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 1
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 1